UNC-39, the C. elegans homolog of the human myotonic dystrophy-associated homeodomain protein Six5, regulates cell motility and differentiation (Q47069426)

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scientific article published in August 2004

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English	UNC-39, the C. elegans homolog of the human myotonic dystrophy-associated homeodomain protein Six5, regulates cell motility and differentiation	scientific article published in August 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

UNC-39, the C. elegans homolog of the human myotonic dystrophy-associated homeodomain protein Six5, regulates cell motility and differentiation (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

Caenorhabditis elegans

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Homeobox protein unc-39 CELE_F56A12.1

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GOA release 2020-03-11

4

object named as

Harald Hutter

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Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

Edward M Hedgecock

3

object named as

Edward Hedgecock

1 reference

Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

author name string

Judith L Yanowitz

1

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Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

M Afaq Shakir

2

1 reference

Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

Andrew Z Fire

5

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Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

Erik A Lundquist

6

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Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

language of work or name

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publication date

1 August 2004

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Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

Developmental Biology

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Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

272

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Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

2

1 reference

Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

389-402

1 reference

Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

The Drosophila sine oculis locus encodes a homeodomain-containing protein required for the development of the entire visual system

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

The Caenorhabditis elegans Six/sine oculis class homeobox gene ceh-32 is required for head morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Genetic control of programmed cell death in the nematode C. elegans.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Analysis of a Caenorhabditis elegans Twist homolog identifies conserved and divergent aspects of mesodermal patterning

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Unstable DNA sequence in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Functions of LIM-homeobox genes.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

The postembryonic cell lineages of the hermaphrodite and male gonads in Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Drosophila homolog of the myotonic dystrophy-associated gene, SIX5, is required for muscle and gonad development.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Altered myogenesis in Six1-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Six3 promotes the formation of ectopic optic vesicle-like structures in mouse embryos

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Mutations affecting embryonic cell migrations in Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Mechanosensory signalling in C. elegans mediated by the GLR-1 glutamate receptor

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

DNA transformation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

A new mutation in the six-domain of SIX3 gene causes holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Expression of myogenin during embryogenesis is controlled by Six/sine oculis homeoproteins through a conserved MEF3 binding site

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Post-embryonic cell lineages of the nematode, Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

The embryonic cell lineage of the nematode Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Characterization of cardiac conduction system abnormalities in mice with targeted disruption of Six5 gene.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

The Structure of the Nervous System of the Nematode Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.05.010

7 January 2021

Identifiers

10.1016/J.YDBIO.2004.05.010

1 reference

Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 January 2018

http://europepmc.org/abstract/MED/15282156

ResearchGate publication ID

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